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Curiteva Sacroiliac Joint Fusion System

Page Type
Cleared 510(K)
510(k) Number
K210402
510(k) Type
Traditional
Applicant
Curiteva, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2021
Days to Decision
211 days
Submission Type
Summary

Curiteva Sacroiliac Joint Fusion System

Page Type
Cleared 510(K)
510(k) Number
K210402
510(k) Type
Traditional
Applicant
Curiteva, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2021
Days to Decision
211 days
Submission Type
Summary